Canonical Allele Identifier: CA2430311503

Gene: MAGED2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54809963C= , CM000685.2:g.54809963C=	GRCh38
NC_000023.10:g.54836396C= , CM000685.1:g.54836396C=	GRCh37
NC_000023.9:g.54853121C=	NCBI36
NG_012844.1:g.7226C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375068.6:c.287C= MANE Select	ENSP00000364209.1:p.Ala96=
ENST00000218439.8:c.287C=	ENSP00000218439.4:p.Ala96=
ENST00000347546.8:c.233C=	ENSP00000336962.4:p.Ala78=
ENST00000375053.6:c.287C=	ENSP00000364193.2:p.Ala96=
ENST00000375058.5:c.287C=	ENSP00000364198.1:p.Ala96=
ENST00000375060.5:c.173C=	ENSP00000364200.1:p.Ala58=
ENST00000375068.5:c.287C=	ENSP00000364209.1:p.Ala96=
ENST00000396224.1:c.287C=	ENSP00000379526.1:p.Ala96=
ENST00000463787.5:n.123-155C=
ENST00000485483.1:n.522C=
ENST00000497484.1:n.430C=
ENST00000627068.2:c.173C=	ENSP00000486563.1:p.Ala58=
NM_014599.5:c.287C=	NP_055414.2:p.Ala96=
NM_177433.2:c.287C=	NP_803182.1:p.Ala96=
NM_201222.2:c.287C=	NP_957516.1:p.Ala96=
NM_177433.3:c.287C= MANE Select	NP_803182.1:p.Ala96=
NM_014599.6:c.287C=	NP_055414.2:p.Ala96=
NM_201222.3:c.287C=	NP_957516.1:p.Ala96=